MULTISTIM
Stimulator, Nerve, Battery-powered
PAJUNK GMBH
The following data is part of a premarket notification filed by Pajunk Gmbh with the FDA for Multistim.
Pre-market Notification Details
| Device ID | K011308 |
| 510k Number | K011308 |
| Device Name: | MULTISTIM |
| Classification | Stimulator, Nerve, Battery-powered |
| Applicant | PAJUNK GMBH 203 MAIN STREET, PMB 166 Flemington,, NJ 08822 |
| Contact | Lynette Howard |
| Correspondent | Lynette Howard PAJUNK GMBH 203 MAIN STREET, PMB 166 Flemington,, NJ 08822 |
| Product Code | BXN |
| CFR Regulation Number | 868.2775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-04-30 |
| Decision Date | 2001-11-29 |
Trademark Results [MULTISTIM]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MULTISTIM 85318436 4511095 Live/Registered |
WELLFIRST TECHNOLOGIES, INC. 2011-05-11 |
 MULTISTIM 85318428 4407472 Live/Registered |
WELLFIRST TECHNOLOGIES, INC. 2011-05-11 |
 MULTISTIM 77913065 not registered Dead/Abandoned |
LOGAN COMPLETION SYSTEMS INC. 2010-01-15 |
 MULTISTIM 73663379 1532864 Live/Registered |
NEUROMED, INC. 1987-05-28 |
 MULTISTIM 73549337 1383256 Dead/Cancelled |
EXCEL-TECH LTD. 1985-07-22 |
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